Persistent unilateral central serous chorioretinopathy in a breastfeeding woman

di Lopez-Yang, Christine Elizabeth, Garcia, Charles A
Pubblicato in BMJ Case Rep (2015)

Pearls of Elschnig

di Foutch, Brian K, Garcia, Charles A, Ferguson, Amy S
Pubblicato in J Ophthalmic Vis Res (2019)

Central serous chorioretinopathy after blunt trauma

di Ponce, Claudia Maria Prospero, Mohidat, Hasan M, Garcia, Charles A
Pubblicazione 2012

ACE2 gene transfer ameliorates vasoreparative dysfunction in CD34(+) cells derived from diabetic older adults

di Joshi, Shrinidh, Montes de Oca, Ildamaris, Maghrabi, Ahmad, Lopez-Yang, Christine, Quiroz-Olvera, Julio, Garcia, Charles A., Jarajapu, Yagna Prasada Rao
Pubblicato in Clin Sci (Lond) (2021)

A Preclinical Safety Study of Human Embryonic Stem Cell-Derived Retinal Pigment Epithelial Cells for Macular Degeneration

di Mazzilli, John L., Snook, Joshua D., Simmons, Ken, Domozhirov, Aleksey Y., Garcia, Charles A., Wetsel, Rick A., Zsigmond, Eva M., Westenskow, Peter D.
Pubblicato in J Ocul Pharmacol Ther (2020)

Prevalence of Disease-Causing Mutations in Families with Autosomal Dominant Retinitis Pigmentosa: A Screen of Known Genes in 200 Families

di Sullivan, Lori S., Bowne, Sara J., Birch, David G., Hughbanks-Wheaton, Dianna, Heckenlively, John R., Lewis, Richard Alan, Garcia, Charles A., Ruiz, Richard S., Blanton, Susan H., Northrup, Hope, Gire, Anisa I., Seaman, Robyn, Duzkale, Hatice, Spellicy, Catherine J., Zhu, Jingya, Shankar, Suma P., Daiger, Stephen P.
Pubblicazione 2006

A Dominant Mutation in Hexokinase 1 (HK1) Causes Retinitis Pigmentosa

di Sullivan, Lori S., Koboldt, Daniel C., Bowne, Sara J., Lang, Steven, Blanton, Susan H., Cadena, Elizabeth, Avery, Cheryl E., Lewis, Richard A., Webb-Jones, Kaylie, Wheaton, Dianna H., Birch, David G., Coussa, Razck, Ren, Huanan, Lopez, Irma, Chakarova, Christina, Koenekoop, Robert K., Garcia, Charles A., Fulton, Robert S., Wilson, Richard K., Weinstock, George M., Daiger, Stephen P.
Pubblicato in Invest Ophthalmol Vis Sci (2014)

North Carolina Macular Dystrophy is caused by dysregulation of the retinal transcription factor PRDM13

di Small, Kent W., DeLuca, Adam P., Whitmore, S. Scott, Rosenberg, Thomas, Silva-Garcia, Rosemary, Udar, Nitin, Puech, Bernard, Garcia, Charles A., Rice, Thomas A., Fishman, Gerald A., Héon, Elise, Folk, James C., Streb, Luan M., Haas, Christine M., Wiley, Luke A., Scheetz, Todd E., Fingert, John H., Mullins, Robert F., Tucker, Budd A., Stone, Edwin. M.
Pubblicato in Ophthalmology (2015)